levoleucovorin calcium(lee-vo-loo-koe-vor-in kal-see-um ) ,
Pregnancy Category: C
Pharmacologic: folic acid analogues
Pharmacologic: folic acid analogues
Used as “rescue” following high-dose methotrexate treatment of osteosarcoma.Decreases toxicity which may follow impaired methotrexate elimination or unintended toxicity of other folic acid antagonists.In combination with 5–fluorouracil for the palliative treatment of advanced metastatic colorectal cancer.
The reduced form of folic acid that serves as a cofactor in the synthesis of DNA and RNA; does not require dihydrofolate reductase for activity.
Reversal of toxic effects of folic acid antagonists, including methotrexate, that inhibit dihydrofolate reductase.
Improved survival and performance status in patients with colorectal cancer.
Absorption: IV administration results on complete bioavailability.
Distribution: Transported actively and passively across cell membranes; enters CSF.
Metabolism and Excretion: Extensively converted to tetrahydrofolic derivatives.
Half-life: Total tetrahydrofolic acid—5.1 hr.
|IV||unknown||end of infusion||3–6 hr|
Contraindicated in: Hypersensitivity to folic acid or folinic acid.
Use Cautiously in: Concurrent use of anticonvulsants; may increase risk of seizures; Obstetric / Lactation: Use in pregnancy only if clearly needed, use cautiously during lactation; Pediatric: Has been used safely.
Adverse Reactions/Side Effects(all patients also received methotrexate)
Central nervous system
- nausea (most frequent)
- stomatitis (most frequent)
- vomiting (most frequent)
- altered taste
- abnormal renal function
- allergic reactions
Drug-Drug interaction↑ risk of toxicity from fluorouracil.May ↓ effectiveness of phenobarbital , phenytoin, or primidone leading to ↑ risk of seizures.May ↓ effectiveness of trimethoprim-sulfamethoxazole when used to treat Pneumocustis carnii pneumonia in HIV-infected patients.
Levoleucovorin Rescue Following High-Dose Methotrexate—based on a methotrexate dose of 12 grams/m2 IV over 4 hr and concurrent with hydration and maintenance of urine pH ≥7.0
Intravenous (Adults) Normal methotrexate elimination—7.5 mg (5 mg/m2) every 6 hr for 10 doses starting 24 hr after the start of the methotrexate infusion; Delayed late methotrexate elimination—7.5 mg (5 mg/m2) every 6 hr starting 24 hr after the start of the methotrexate infusion; continue until methotrexate level <5 × 10–8 (0.05 micromolar); delayed early methotrexate elimination and/or evidence of acute renal injury—75 mg (5 mg/m2) every 3 hr starting 24 hr after the start of the methotrexate infusion; continue until methotrexate level is <1 micromolar, then 7.5 mg every 3 hr until 0.05 micromolar).
Levoleucovorin Rescue Following Inadvertent Overdosage of Methotrexate
Intravenous (Adults) 7.5 mg (approximately 5 mg/m2) every 6 hr until serum methotrexate level is less than 10−8 M. Determine creatinine and methotrexate levels at 24 hr intervals. If 24 hour serum creatinine has increased 50% over baseline or 24 hr methotrexate level is greater than 5 × 10−6 M or 48 hr level is greater than 9 × 10−7 M, ↑ dose to 50 mg/m2 IV every 3 hr until methotrexate level is less than 10−8 M. Maintain hydration and urinary alkalinization (pH ≥7.0). Initiate as soon as possible and within 24 hr of methotrexate when there is delayed excretion; as time interval increases, effectiveness ↓.
Palliative Treatment of Advanced Metastatic Colorectal Cancer (in combination with 5–fluorouracil)
Intravenous (Adults) 100 mg/m2 followed by 5–fluorouracil 370 mg/m2; regimen should be given daily for 5 days; repeat regimen q 4 wk for 2 courses (may then repeat course q 4–5 wk if patient tolerates)or levoleucovorin 10 mg/m2 followed by 5–fluorouracil 425 mg/m2; regimen should be given daily for 5 days; repeat regimen q 4 wk for 2 courses (may then repeat course q 4–5 wk if patient tolerates).
Lyophylized powder for injection (requires reconstitution: 50 mg/vial (contains mannitol)
Solution for injection: 10 mg/mL
- Assess patient for nausea and vomiting secondary to methotrexate therapy or folic acid antagonists (pyrimethamine and trimethoprim) overdose.
- Monitor for development of allergic reactions (rash, urticaria, wheezing). Notify health care professionalif these occur.
- Lab Test Considerations: Monitor serum methotrexate and creatinine at least once daily levels to determine dosage and effectiveness of therapy. Leucovorin calcium levels should be equal to or greater than methotrexate level. Rescue continues until serum methotrexate level is <5 × 10−8 M.
- Monitor electrolytes and hydration status, and urine pH every 6 hr during therapy; pH should be maintained >7 to decrease nephrotoxic effects of high-dose methotrexate.
Potential Nursing DiagnosesRisk for injury (Indications)
Imbalanced nutrition: less than body requirements (Indications)
- Levoleucovorin is dosed at one-half the usual dose of the racemic form.
- Intermittent Infusion: Reconstitute 50 mg vial with 5.3 mL of 0.9% NaCl without preservatives for a concentration of 10 mg/mL. Diluent: Dilute further immediately with 0.9% NaCl or D5W. Concentration: 0.5 mg/mL–5 mg/mL. Initial reconstitution or dilutions in 0.9% NaCl are stable at room temperature for 12 hr. Dilutions in D5W are stable for 4 hrs at room temperature. Do not administer solutions that are cloudy or contain a precipitate.
- Rate: Administer at no more than 16 mL of reconstituted solution (160 mg levoleucovorin) per min; due to calcium content of solution.
- Additive Incompatibility: Do not admix with other solutions.
- Explain purpose of medication to patient.
- Reversal of toxic effects of methotrexate or in overdose of folic acid antagonists.
Drug Guide, © 2015 Farlex and Partners